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A Method to Assess Fc-mediated Effector Functions Induced by Influenza Hemagglutinin Specific Antibodies
Published on: February 23, 2018
T helper cells and efficacy of Haemophilus influenzae type b conjugate vaccination
Jodie McVernon1, N Avrion Mitchison, E Richard Moxon
1Immunisation Department, Health Protection Agency, Communicable Disease Surveillance Centre, London, UK. jodie.mcvernon@hpa.org.uk
Insights
Fully vaccinated children in the UK are experiencing invasive Haemophilus influenzae type b (Hib) infections. This rise may stem from the conjugate vaccine
Area of Science:
- Immunology
- Vaccinology
- Infectious Diseases
- Public Health
Background:
- Invasive Haemophilus influenzae type b (Hib) infections are occurring in a small number of fully vaccinated children in the UK.
- Recent years have seen a rise in Hib disease, linked to declining vaccine-induced antibody levels in early childhood.
- Protection increasingly relies on immunological memory, necessitating interventions like catch-up vaccination campaigns.
Purpose of the Study:
- To investigate the reasons behind the resurgence of invasive Hib infections in vaccinated UK children.
- To explore the potential role of vaccine-induced immune responses and natural boosting in disease incidence.
- To assess the implications for current and future conjugate vaccine strategies.
Main Methods:
- Analysis of invasive Hib infection cases in fully vaccinated children.
- Evaluation of vaccine-induced antibody levels and immunological memory.
- Assessment of Hib circulation patterns and potential impact on natural boosting.
Main Results:
- A rise in invasive Hib infections observed in fully vaccinated children.
- Lower vaccine-induced antibody levels noted in the first five years of life.
- Potential contribution of impaired T cell response and reduced natural boosting to increased disease incidence.
Conclusions:
- The conjugate vaccine's limitations in inducing specific helper T cells and reduced natural boosting may contribute to rising invasive Hib disease.
- The findings suggest that the vaccine may not fully activate all necessary immune system components.
- This has significant implications for the scheduling and design of other conjugate vaccines, including those for meningococcal and pneumococcal diseases.
Abstract:
A small number of fully vaccinated children in the UK have experienced invasive Haemophilus influenzae type b (Hib) infection. A rise in disease in recent years has been associated with lower vaccine-induced antibody levels over the first 5 years of life, forcing greater dependence on immunological memory for protection. This has necessitated the introduction of a catch-up campaign, designed to boost immunity in children aged 6 months to 4 years of age. We suggest that the conjugate vaccine's inability to induce pathogen specific helper T cells, combined with a loss of natural boosting due to reduced circulation of Hib, may have contributed to the rising incidence of invasive disease 10 years after introduction of the conjugate vaccine. If so, the changing epidemiology of Hib infection in the UK may in part reflect the failure of a subunit vaccine to activate adequately all the necessary components of the immune system. This observation has implications for optimal scheduling of more recently licensed meningococcal and pneumococcal conjugate vaccines.
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